Combined auxiliary diagnostic method, kit, system and use of point mutation and methylation of bladder cancer driver genes

ABSTRACT

Disclosed are the method, kit, system and use for screening or detecting or assisting in the diagnosis of bladder cancer, which are able to simultaneously detect FGFR3, TERT, PLEKHS1 point mutations and OTX1, NID2 and NRN1 methylation levels, thereby realizing the combined detection of gene point mutation and methylation, reducing the demand for samples, experimental operation steps and detection cycle, and improving the specificity and sensitivity of detection.

CROSS REFERENCE TO RELATED APPLICATION

This patent application claims the benefit and priority of Chinese Patent Application NO. 201910988473.X entitled “Combined auxiliary diagnostic method, kit, system and use of point mutation and methylation of bladder cancer driver genes” filed on Oct. 17, 2019, the disclosure of which is incorporated by reference herein in its entirety as part of the present application.

TECHNICAL FIELD

The present disclosure belongs to the technical field of gene mutation detection, and particularly relates to a method for simultaneously detecting DNA methylation and single nucleotide polymorphism of bladder cancer driver genes, a related kit, a system and use thereof.

BACKGROUND ART

Bladder cancer is the most common malignant tumor of urinary system, ranking the sixth in the incidence of male tumors in China. Among them, the incidence rate of male is 3-4 times that of female, while the mortality rate of female is higher than that of male. Bladder cancer becomes an adult cancer with the highest diagnosis and treatment cost due to the need for continuous follow-up and high recurrence rate after surgery (the recurrence rate of non muscle-invasive bladder cancer can reach 60-70%).

Poor prognosis and easy recurrence are important characteristics of bladder cancer, and effective treatment largely depends on early diagnosis and early treatment of bladder cancer. However, the incidence of early bladder cancer is asymptomatic, and most patients only go to the hospital because of hematuria under the naked eye or microscope, and they have already been at an advanced stage of cancer at that time. Therefore, it is of great clinical value to find a specific early diagnosis method for bladder cancer. Cystoscopy, as the gold standard for the diagnosis of bladder cancer, has a missed diagnosis rate of up to 10%, and it is an invasive examination with low acceptance. Urine cytology has high sensitivity to high-grade bladder cancer, but low detection rate to low-grade bladder cancer. Imaging tests may detect larger tumors in the bladder. However, none of the traditional bladder cancer examination methods mentioned above can meet the requirements of non-invasive and high detection rate at the same time.

Although molecular diagnostic methods can diagnose bladder cancer in clinic at present, they are all singly used. For example, the method is only for detecting gene methylation or single point mutation and other relevant biological information. The accuracy and sensitivity of its detection rate are still unsatisfactory.

In view of the above problems, the combined detection of point mutation and methylation of driver gene is used for the first time in the present disclosure to diagnose bladder cancer, improving the shortcoming of single detection of the current detection method, comprehensively evaluating the negative and positive of detection samples from multiple dimensions, and greatly expanding the detection area, and thus screening bladder cancer tumorigenesis at an early stage. Therefore, the development of diagnostic technology based on this product is of great significance for preventing bladder cancer and monitoring postoperative recurrence.

SUMMARY OF THE INVENTION

In view of this, the purpose of the present disclosure is to provide a method for simultaneously detecting DNA methylation and single nucleotide polymorphism of bladder cancer driver genes, a related kit, a system and use thereof. The detection method, related kit and system have characterized with good sensitivity and high accuracy, and greatly improve the detection rate of bladder cancer in the early stage.

In order to achieve the purpose of the present disclosure, the present disclosure provides a detection method for screening bladder cancer by targeting genes related to the pathway of bladder cancer, which comprises the detection for targeting gene point mutation and/or methylation level of gene expression regulatory region. In some embodiments, the detection method is the combined detection for targeting gene point mutation and methylation level of gene regulatory region.

In some embodiments, the genes for detecting point mutation include one or more combinations of FGFR3, TERT and PLEKHS1. In some embodiments, the region to be detected for point mutation in FGFR3 is set forth in SEQ ID NO: 1; the region to be detected for TERT point mutation is set forth in SEQ ID NO: 2; and the region to be detected for PLEKHS1 point mutation is set forth in SEQ ID NO: 3. In some embodiments, the genes for detecting the methylation level in regulatory region include one or more combinations of OTX1, NID2 and NRN1. In some embodiments, the region to be detected for OTX1 methylation level is set forth in SEQ ID NO: 4; the region to be detected for NID2 methylation level is set forth in SEQ ID NO: 5; the region to be detected for NRN1 methylation level is set forth in SEQ ID NO: 6.

In some embodiments, the detection method also includes the detection of internal reference genes. In some embodiments, the internal reference gene is ATCB. In some embodiments, the primers and probe of ATCB are the sequences set forth in SEQ ID NO: 41-SEQ ID NO: 43.

The present disclosure also provides a detection reagent for screening bladder cancer by targeting genes related to the pathway of bladder cancer, which comprises specific primers and probes designed for a template of the region to be detected, detecting by using a fluorescent quantitative PCR instrument through a PCR reaction system, thereby realizing the detection for samples.

In some embodiments, the designed specific primers include a forward primer and a reverse primer designed for the region to be detected. In some embodiments, the region to be detected includes point mutation and gene methylation. In some embodiments, the gene methylation sites in the region to be detected include a CpG site. In some embodiments, the point mutation comprises a point mutation for one or more combinations of FGFR3, TERT and PLEKHS1. In some embodiments, the region to be detected for FGFR3 point mutation is the sequence set forth in SEQ ID NO: 1; the region to be detected for TERT point mutation is the sequence set forth in SEQ ID NO: 2; and the region to be detected for PLEKHS1 point mutation is the sequence set forth in SEQ ID NO: 3.

In some embodiments, the gene methylation comprises methylation for one or more combinations of OTX1, NID2 and NRN1.

In some embodiments, the region to be detected for OTX1 methylation is the sequence set forth in SEQ ID NO: 4; the region to be detected for NID2 methylation level is the sequence set forth in SEQ ID NO: 5; the region to be detected for NRN1 methylation level is the sequence set forth in SEQ ID NO: 6.

In some embodiments, the size of the forward primer and the reverse primer amplification of the target region is 80-150 bp, preferably 80-100 bp. In some embodiments, the 3′ end of the forward primer or the reverse primer overlap with the site to be detected. In some embodiments, the point to be detected is 0-5 bases away from the 3′ end of the forward primer or the reverse primer. In some embodiments, 0-2 base mismatches are introduced into the penultimate position and the antepenultimate position at the 3′ end of the detection primer, so as to improve the specificity of the detection mutation template of the primer. In some embodiments, the 0-2 base mismatches of the penultimate primer and the antepenultimate primer at the 3′ end of the detection primer follow the mismatch combination of strong mismatch plus weak mismatch or weak mismatch plus strong mismatch combinations. In some embodiments, the strong mismatch base is A/G and C/T. In some embodiments, the weak mismatch base is: A/C and G/T. In some embodiments, the detection primers can be selected from the sequences set forth in SEQ ID NOs: 7-11, 13-17, 19-23, 25-29, 31-34 and 36-39. In some embodiments, the forward primers and reverse primers for FGFR3 point mutation may be selected from any sequence set forth in SEQ ID NOs: 7-10 as well as the sequence set forth in SEQ ID NO: 11, preferably the forward primer and reverse primer are the sequences set forth in SEQ ID NO: 10 and SEQ ID NO: 11, respectively. In some embodiments, the forward primers and reverse primers for TERT point mutation may be selected from any sequence set forth in SEQ ID NOs: 13-16 as well as the sequence set forth in SEQ ID NO: 17; preferably, the forward primer and reverse primer are set forth in SEQ ID NO: 16 and SEQ ID NO: 17 respectively. In some embodiments, the forward primers and reverse primers for PLEKHS1 point mutation are selected from any sequence set forth in SEQ ID NOs: 19-22 as well as the sequence set forth in SEQ ID NO: 23; and preferably the forward primer and reverse primer are the sequences set forth in SEQ ID NO: 22 and SEQ ID NO: 23 respectively. In some embodiments, the forward primers and reverse primers for OTX1 methylation may be selected from any sequence set forth in SEQ ID NOs: 25 and 26 and any of the sequence set forth in SEQ ID NOs: 27-29; preferably the forward primer and reverse primer are the sequences set forth in SEQ ID NO: 25 and SEQ ID NO: 29, respectively. In some embodiments, the forward primers and reverse primers for NID2 methylation may be selected from the sequence set forth in SEQ ID NO: 31 as well as any one of the sequence set forth in SEQ ID NOs: 32-34; preferably the forward primer and reverse primer are the sequences set forth in SEQ ID NO: 31 and SEQ ID NO: 34, respectively. In some embodiments, the forward primers and reverse primers for NRN1 methylation may be selected from the sequences set forth in SEQ ID NO: 36 as well as any of the sequence set forth in SEQ ID NO: 37-39, and preferably the forward primer and reverse primer are the sequences set forth in SEQ ID NO: 36 and SEQ ID NO: 39, respectively. In some embodiments, the probe is close to the site to be detected. In some embodiments, the probe is close to the site to be detected. In some embodiments, the probe reporter fluorophores include one or more probe reporter fluorophores such as FAM, HEX, VIC and ROX. The quenchers include one or more quenchers such as BHQ1, BHQ2, Cy3 and Cy5. In some embodiments, the probe is selected from any sequence set forth in SEQ ID NOs: 12, 18, 24, 30, 35 and 40 or any combination thereof. In some embodiments, the templates of the region to be detected include DNA templates and single-stranded templates after heavy salt transformation; preferably a template after heavy salt transformation. In some embodiments, the heavy salt transformation is carried out by bisulfite. In some embodiments, the structure of the region to be detected is selected from any sequence set forth in SEQ ID NOs: 1-6 or any combination thereof. In some embodiments, the specific primers and probes also include primers and probes designed for internal reference genes. In some embodiments, the internal reference gene is selected from ATCB. In some embodiments, the primer and probe designed for the internal reference gene are set forth in SEQ ID NOs: 41, 42 and 43.

In addition, the present disclosure also provides an efficient and highly specific PCR reaction system for screening bladder cancer by targeting genes related to the pathway of bladder cancer. The PCR reaction system comprises the primers and probes, PCR reaction enzymes and PCR enhancers, which are used for screening bladder cancer by targeting genes related to the pathway of bladder cancer.

In some embodiments, the PCR reaction enzyme is selected from DNA polymerases with 5′-3′ exonuclease activity: such as one or more of Taq DNA polymerase, AmpliTaq Gold 360 DNA polymerase and 2G Robust DNA polymerase.

In some embodiments, the PCR enhancer comprises: 1-10 mM DTT, 0.1-10% DMSO and 1-5% glycerol.

In addition, the present disclosure also provides a PCR detection reaction procedure for screening bladder cancer by targeting the genes related to the pathway of bladder cancer, which is used for the detection method and detection reagent for screening bladder cancer by targeting genes related to the pathway of bladder cancer, and the detection procedure comprises three modules: a sample denaturation reaction module, a high TM region template pre-amplification enrichment module and a detection reaction module. In some embodiments, the sample denaturation reaction module realizes the denaturation of the sample into a single chain. In some embodiments, the high TM region template pre-amplification enrichment module preferentially amplifies and enriches the mutant template. In some embodiments, the detection reaction module realizes the collection of PCR and fluorescence signals of the sample, and realizes the detection of the sample.

In some embodiments, the preferred PCR detection reaction procedure is as follows:

the first stage 95° C. 10 min 1 cycle pre-denaturation the second 95° C. 15 s 15 cycles high TM template stage 59° C. 45 s enrichment 72° C. 1 min the third stage 95° C. 15 s 35 cycles 55° C. 45 s 72° C. 1 min collection of the fluorescence signal the fourth stage 40° C. 1 min 1 cycle cooling

In addition, the present disclosure also provides an auxiliary diagnostic kit for bladder cancer, which comprises a sample nucleic acid extraction reagent module, a nucleic acid DNA heavy salt transformation module and a point mutation and methylation detection module of bladder cancer driver genes. In some embodiments, the sample is preferably a urine sample. In some embodiments, the nucleic acid extraction module is selected from one or more of Genomic DNA Extraction kit (Genmagbio), Free DNA extraction kit (TIANGEN BIOTECH (BEIJING) CO.,LTD) and Genomic DNA Extraction kit (TIANGEN BIOTECH (BEIJING) CO.,LTD). In some embodiments, the heavy salt transformation is carried out by bisulfite. In some embodiments, the nucleic acid DNA heavy salt transformation module is selected from one or more of large-volume nucleic acid heavy salt transformation kit (TIANGEN BIOTECH (BEIJING) CO.,LTD) and nucleic acid heavy salt transformation kit (Zymo Research). In some embodiments, the point mutation and methylation detection module of bladder cancer driver genes comprises the aforementioned detection reagent for screening bladder cancer by targeting the genes related to the pathway of bladder cancer.

In addition, the present disclosure also provides a detection method using the bladder cancer auxiliary diagnosis kit, which comprises the following steps: 1) extracting nucleic acid from the collected samples; 2) distributing the extracted nucleic acid into two parts, one part is used for heavy salt transformation, and the other part is used for gene point mutation detection, carrying out heavy salt transformation by bisulfite on the nucleic acid sample used for heavy salt transformation; 3) respectively detecting the point mutation and gene methylation level of the part used for gene point mutation detection and the part treated by heavy salt transformation; 4) analyzing the negative and positive of the detection results. In some embodiments, the method may also be as follows: 1) extracting the sample nucleic acid; 2) distributing the extracted nucleic acid into two parts, one part is used for heavy salt transformation, and the other part is used for gene point mutation detection; 3) carrying out heavy salt transformation on the nucleic acid sample used for heavy salt transformation; 4) respectively detecting the point mutation and gene methylation level of the part used for gene point mutation detection and the part treated by heavy salt transformation; 5) analyzing the negative and positive of the detection results. In some embodiments, the heavy salt transformation is carried out by bisulfite. In some embodiments, the collected sample is urine.

In addition, the present disclosure also provides a detection system for screening bladder cancer by targeting the genes related to the pathway of bladder cancer, which is used for performing the following steps: 1) extracting the sample nucleic acid; 2) distributing the extracted nucleic acid into a point mutation detection reaction module and a methylation detection reaction module, carrying out heavy salt transformation treatment on the nucleic acid in the methylation detection reaction module; 3) respectively detecting the point mutation and gene methylation level on the point mutation detection reaction module and the methylation detection reaction module treated by heavy salt transformation; 4) analyzing the negative and positive of the detection results. The detection system for screening bladder cancer by targeting the genes which is related to the pathway of bladder cancer may also be a detection system for performing the following steps: 1) extracting the sample nucleic acid; 2) distributing the extracted nucleic acid into a point mutation detection reaction module and a methylation detection reaction module; 3) carrying out heavy salt transformation treatment on the nucleic acid in the methylation detection reaction module; 4) respectively detecting the point mutation and gene methylation level on the point mutation detection reaction module and the methylation detection reaction module treated by heavy salt transformation; 5) analyzing the negative and positive of the detection results. In some embodiments, the sample may be a urine sample. In some embodiments, the detection system also comprises a module for carrying out the internal reference gene detection. In some embodiments, the point mutation genes include one or more combinations of FGFR3, TERT and PLEKHS1. In some embodiments, the methylated genes include one or more combinations of OTX1, NID2 and NRN1. In some embodiments, the point mutation and gene methylation level are detected by specific primers and probes. In some embodiments, the target region by the specific primers and probes is 80-150 bp, preferably 80-100 bp. In some embodiments, the structure of the region to be detected which is targeted by the specific primers and probes is selected from any one of the sequences set forth in SEQ ID NOs: 1-6 or any combination thereof. In some embodiments, the 3′ end of the forward primer or the reverse primer overlap with the site to be detected. In some embodiments, the point to be detected is 0-5 bases away from the 3′ end of the forward primer or the reverse primer. In some embodiments, 0-2 base mismatches are introduced into the penultimate position and the antepenultimate position at the 3′ end of the detection primer, so as to improve the specificity of the detection mutation template of the primer. In some embodiments, the specific primers can be selected from the sequences set forth in SEQ ID NOs: 7-11, 13-17, 19-23, 25-29, 31-34 and 36-39. In some embodiments, the forward primers and reverse primers for FGFR3 point mutation may be selected from any sequence of SEQ ID NOs: 7-10 as well as the sequence set forth in SEQ ID NO: 11, preferably the forward primer and reverse primer are the sequences set forth in SEQ ID NO: 10 and SEQ ID NO: 11, respectively. In some embodiments, the forward primers and reverse primers for TERT point mutation may be selected from any sequence of SEQ ID NOs: 13-16 as well as the sequence set forth in SEQ ID NO: 17, preferably, the forward primer and reverse primer are set forth in SEQ ID NO: 16 and SEQ ID NO: 17 respectively. In some embodiments, the forward primers and reverse primers for PLEKHS1 point mutation are selected from any sequences set forth in SEQ ID NOs: 19-22 as well as SEQ ID NO: 23, and preferably the forward primer and reverse primer are the sequences set forth in SEQ ID NO: 22 and SEQ ID NO: 23 respectively. In some embodiments, the forward primers and reverse primers for OTX1 methylation may be selected from any sequence set forth in SEQ ID NOs: 25 and 26 and any of the sequences shown in SEQ ID NOs: 27-29, preferably the forward primer and reverse primer are the sequences set forth in SEQ ID NO: 25 and SEQ ID NO: 29, respectively. In some embodiments, the forward primers and reverse primers for NID2 methylation may be selected from the sequences set forth in SEQ ID NO: 31 as well as any one of the sequences set forth in SEQ ID NOs: 32-34, preferably the forward primer and reverse primer are the sequences set forth in SEQ ID NO: 31 and SEQ ID NO: 34, respectively. In some embodiments, the forward primers and reverse primers for NRN1 methylation may be selected from the sequences set forth in SEQ ID NO: 36 as well as any of the sequences set forth in SEQ ID NO: 37-39, and preferably the forward primer and reverse primer are the sequences set forth in SEQ ID NO: 36 and SEQ ID NO: 39, respectively. In some embodiments, the probe is close to the site to be detected. In some embodiments, the probe is close to the site to be detected. In some embodiments, the probe reporter fluorophores include one or more probe reporter fluorophores such as FAM, HEX, VIC and ROX. The quenchers include one or more quenchers such as BHQ1, BHQ2, Cy3 and Cy5. In some embodiments, the probe is selected from any sequence set forth in SEQ ID NOs: 12, 18, 24, 30, 35 and 40 or any combination thereof. In some embodiments, the internal reference gene is ATCB. In some embodiments, the primer and probe designed for the internal reference gene are set forth in SEQ ID NOs: 41, 42 and 43.

In some embodiments, the PCR reaction conditions for detecting the point mutation and the gene methylation level are as follows:

The first stage 95° C. 10 min  1 cycle Pre-denaturation The second stage 95° C. 15 s 15 cycles High TM template 59° C. 45 s enrichment 72° C.  1 min The third stage 95° C. 15 s 35 cycles 55° C. 45 s 72° C.  1 min Collection of the fluorescence signal The fourth stage 40° C.  1 min  1 cycle Cooling

In addition, the present disclosure also provides use of the primers, probes, detection reagents, diagnostic kits and detection systems in preparing products for diagnosis or auxiliary diagnosis of bladder cancer.

Compared with the prior art, the present disclosure has the following beneficial effects:

1) The combined detection of gene point mutation and methylation is realized in the present disclosure, and two kinds of templates are needed according to different types of the site mutation to be detected, thereby reducing the demand for samples, experimental operation steps and detection cycle.

2) The detection reaction procedure is ingeniously designed in the present disclosure, ensuring the stability and detection limit of the detection system, and avoiding false positives caused by amplification of wild type templates.

3) The combined detection of point mutation and methylation of driver gene is ingeniously used in the present disclosure, evaluating the negative and positive of samples from two dimensions, and improving the specificity and sensitivity of detection.

DETAILED DESCRIPTION OF THE EMBODIMENTS Example 1 Preparation of the Combined Auxiliary Diagnostic Kit of Gene Point Mutation and Methylation of the Bladder Cancer Driver Genes

1. Design of primers and probes 1) Point mutation targets, primers and probes of driver genes FGFR3 exon7 (SEQ ID NO: 1) GTGCTGGGTGAGGGCCCTGGGGCGGCGCGGGGGTGGGGGCGGCAGTGG CGGTGGTGGTGAGGGAGGGGGTGGCCCCTGAGCGTCATCTGCCCCCACAGAG CGCT[C]CCCGCACCGGCCCATCCTGCAGGCGGGGCTGCCGGCCAACCAGACG GCGGTGCTGGGCAGCGACGTGGAGTTCCACTGCAAGGTGTACAGTGACGCAC AGCCCCACATCCAGTGGCTCAAGCACGTGGA c.746C>G After heavy salt transformation: GTGTTGGGTGAGGGTTTTGGGGCGGCGCGGGGGTGGGGGCGGTAGTGG CGGTGGTGGTGAGGGAGGGGGTGGTTTTTGAGCGTTATTTGTTTTTATAGAGC GTTMTTCGTATCGGTTTATTTTGTAGGCGGGGTTGTCGGTTAATTAGACGGCG GTGTTGGGTAGCGACGTGGAGTTTTATTGTAAGGTGTATAGTGACGTATAGTTT TATATTTAGTGGTTTAAGTACGTGGA FGFR3-ARMS-F1: (SEQ ID NO: 7) GAGCGTTATTTGTTTTTATAGAGCGTTG FGFR3-ARMS-F2: (SEQ ID NO: 8) TTGAGCGTTATTTGTTTTTATAGAGCGTTGT FGFR3-ARMS-F3: (SEQ ID NO: 9) GAGCGTTATTTGTTTTTATAGAGCGTTGTT FGFR3-ARMS-F4: (SEQ ID NO: 10) GAGCGTTATTTGTTTTTATAGAGCGGTG FGFR3-ARMS-R: (SEQ ID NO: 11) TAAAACTATACGTCACTATACACCTTAC FGFR3-ARMS-FAM: (SEQ ID NO: 12) CGTATCGGTTTATTTTGTAGGCGGGGTTGTCG TERT promoter (SEQ ID NO: 2) GCTTCCCACGTGCGCAGCAGGACGCAGCGCTGCCTGAAACTCGCGCCGC GAGGAGAGGGCGGGGCCGCGGAAAGGAAGGGGAGGGGCTGGGAGGGCCCG GAGGGGGCTGGGCCGGGGACCCGG[G]AGGGGTCGGGACGGGGCGGGGTCCG CGCGGAGGAGGCGGAGCTGGAAGGTGAAGGGGCAGGACGGGTGCCCGGGTC CCCAGTCCCTCCGCCACGTGGGAAG c.1-146C>T After heavy salt transformation: GTTTTTTACGTGCGTAGTAGGACGTAGCGTTGTTTGAAATTCGCGTCGCG AGGAGAGGGCGGGGTCGCGGAAAGGAAGGGGAGGGGTTGGGAGGGTTCGGA GGGGGTTGGGTCGGGGATTCGG[G]AGGGGTCGGGACGGGGCGGGGTTCGCGC GGAGGAGGCGGAGTTGGAAGGTGAAGGGGTAGGACGGGTGTTCGGGTTTTTA GTTTTTTCGTTACGTGGGAAG TERT-ARMS-F1: (SEQ ID NO: 13) GAGGGGGTTGGGTCGGGGATTCGGA TERT-ARMS-F2: (SEQ ID NO: 14) GGGTTGGGTCGGGGATTCGGAA TERT-ARMS-F3: (SEQ ID NO: 15) GGTTGGGTCGGGGATTCGGAAG TERT-ARMS-F4: (SEQ ID NO: 16) GAGGGGGTTGGGTCGGGGATTCTGA TERT-ARMS-R: (SEQ ID NO: 17) CCGAACACCCGTCCTACCCCTTCA TERT-ARMS-HEX: (SEQ ID NO: 18) TCGGGACGGGGCGGGGTTCGCG PLEKHS1 (SEQ ID NO: 3) GAGCACTGGACCAGCGACCTCTTGGCTTCCAGTAAGTACTGCTTGGTGTA TCTGGTTTGGACTTCCAAGGCTGGGATGATCTAGAAGCTTTTTTGCAATT[G]AA CAATTGCAAAATTGGAAATGGAAAATTTTGCAGATATGCTGTATTTCTGTTATGG GCACTTTCTTCATAAGCTTCCTAGGCTATACTATAGTCAGAGGGAA After heavy salt transformation: GAGTATTGGATTAGCGATTTTTTGGTTTTTAGTAAGTATTGTTTGGTGTATT TGGTTTGGATTTTTAAGGTTGGGATGATTTAGAAGTTTTTTTGTAATT[G]AATAA TTGTAAAATTGGAAATGGAAAATTTTGTAGATATGTTGTATTTTTGTTATGGGTA TTTTTTTTATAAGTTTTTTAGGTTATATTATAGTTAGAGGGAA G>A PLEKHS1-ARMS-F1: (SEQ ID NO: 19) GATGATTTAGAAGTTTTTTTGTAATTA PLEKHS1-ARMS-F2: (SEQ ID NO: 20) GATGATTTAGAAGTTTTTTTGTAATTAA PLEKHS1-ARMS-F3: (SEQ ID NO: 21) GGATGATTTAGAAGTTTTTTTGTAATTAAA PLEKHS1-ARMS-F4: (SEQ ID NO: 22) GATGATTTAGAAGTTTTTTTGTAAGTA PLEKHS1-ARMS-R: (SEQ ID NO: 23) CTTATAAAAAAAATACCCATAACAAAAATAC PLEKHS1-ARMS-ROX: (SEQ ID NO: 24) TAAAATTGGAAATGGAAAATTTTGTAGATATG 2) Driver gene methylation templates, primers and probes >OTX1 Methylation site template: (SEQ ID NO: 4) CGTTTGGAGGTTTTTTGATTTGTTTTTATATTTAATTTTGTGTAAATTTTTTA TTTCGTTTGTCGGGGTGGGGGAGTGGGGGAGATTAGAAATAAGGGGTAGAAAT TTTT[CG]AAAGGGAATAAAGTGTTTAATTTTTAGGAGGAGGTGTTATTTAAAAG ATT[CG]TTTAGTTTAGAGTTGGTTT[CG]GGTGGGAAATGGGTTT[CG]TT[CG]TA CG+AATAATT[CG]GGGAAAT[CG]TTTTAAGGAGGATTTTTA[CG]TAGTATGTGGA AAAAAGTTGAGGGTAGGGGTTTGTGGTTATATTTTTTATTAAAAAGTTTTTGTT AGAGGTAGTTTAAGAAAGAGAGAGAAAGAGCGAAAAAGAAATTTTT OTX1-bis-ARMS-F1: (SEQ ID NO: 25) CGTTTAGTTTAGAGTTGGTTTCG OTX1-bis-ARMS-F2: (SEQ ID NO: 26) AGTTTAGAGTTGGTTTCGGG OTX1-bis-ARMS-R1: (SEQ ID NO: 27) CTACGTAAAAATCCTCCTTAAAACG OTX1-bis-ARMS-R2: (SEQ ID NO: 28) CTACGTAAAAATCCTCCTTAAAAC OTX1-bis-ARMS-R3: (SEQ ID NO: 29) CTACGTAAAAATCCTCCTTAAATCG OTX1-bis-ARMS-FAM: (SEQ ID NO: 30) ATGGGTTTCGTTCGTACGAATAA >NID2 (SEQ ID NO: 5) GTAGTGGTTATTATATTTGGTTTTCGTTAATTTTTTTAAGGTAGCGGTCGTT GGAGTAGCGGGGTTGGCGGGGTAAAAGTTTTTGGTTAGGGTTGTTTGGAGTTG TTTTTTTTATTT[CG]TTTTTAGGGAGTTTT[CG]GGTTATTTTTTTATT[CG]GGTTG TTT[CG][CG]GTTTTTAAGGAGTTTTATTTT[CG]GGATTAAATGGTT[CG]TAAGGT TTGGGGTAG[CG]G[CG]TTGTAGGAGATGAGTTTAG[CG]TAAAGGGAATTT[CG] TAGCGGCGAGTGCGGTTGTTGGTTTGCGCGTTGTGGTTTTAATAGGTTGGTAGG GCGCGGGCGGGTGGCGGGGTTGCGGTATGAGTTTTGTTTTTTGTTTTG NID2-bis-ARMS-F1: (SEQ ID NO: 31) GGTTAGGGTTGTTTGGAGTTGT NID2-bis-ARMS-R1: (SEQ ID NO: 32) CAAACCTTACGAACCATTTAATCCC NID2-bis-ARMS-R2: (SEQ ID NO: 33) CAAACCTTACGAACCATTTAATACC NID2-bis-ARMS-R3: (SEQ ID NO: 34) CAAACCTTACGAACCATTTAATCAC NID2-bis-ARMS-HEX: (SEQ ID NO: 35) CGGGTTGTTTCGCGCGGTTTTTAAGGAG NRN1 (SEQ ID NO: 6) TCGGGAGGATCGGATATTTTAATTTTTCGGTTTTTAACGCGGGCGTTTGTT CGCGAGCGTCGGGTTAGACGTCGAAGAGGAAGGTGATCGAATTCGTAGTAGTT TTCGAGAGCGTATTCGTTTGTAAATTGTTGTAGGAAGAG+CQAGG[CG]GGTTT TG[CG]TTTTTTAATT[CG]GAA[CG]GGAAGTATTGGGGAAGGGAT[CG]AGGTTA ATTT[CG]ATTTT[CG]TTGGGGTAGATA[CG]TAAATTTTTTTAAATTTT[CG]AGTT TATTT TATAG[CG]AATATTAAATATTTTTG[CG]ATTATAATATTAATAAATCGAATA TTGA[CG]TAAAATTTTAAGAATAAACGAATTTTT NRN1-bis-ARMS-F1: (SEQ ID NO: 36) GTTTGTAAATTGTTGTAGGAAGCGC NRN1-bis-ARMS-ROX: (SEQ ID NO: 37) ATCGAAATTAACCTCGATCCCTTCC NRN1-bis-ARMS-R2: (SEQ ID NO: 38) ATATTCGCTATAAAATAAACCCG NRN1-bis-ARMS-R3: (SEQ ID NO: 39) CGTTTATTCTTAAAATTTTCCG NRN1-bis-ARMS-R1: (SEQ ID NO: 40) ATAATCGCAAAAATATTTAATATCCG The above [ ] area was the detection site. 3) ATCB gene primers and probes ATCB-BIS-F2: (SEQ ID NO: 41) AGTGAGAAAGGGTGTAGTTTTGGGAG ATCB-BIS-R3: (SEQ ID NO: 42) CCACAAAAAAATAACCCAAATAAATAACCCACT ATCB-VIC: (SEQ ID NO: 43) CCTCTTCTAATAACCACCTCCCTCCTTCCTAAC

2. Preparation and Composition of Kit

The main components of the urine bladder cancer driver gene point mutation methylation combined detection kit of the present disclosure comprises the following components:

reagent name main components primer & probe A mixture of three driver gene point mutations, internal reference primer and probe primer & probe B mixture of three driver gene methylation, internal reference primer and probe Gold 360 Master Mix DNA polymerase, Mg²⁺

 dN(15)TPs

PCR enhancer DTT and BSA point mutation positive adenovirus packaging positive mutant quality control plasmid methylation positive methylation-positive nucleic acid after quality control methylase transformation negative control T cells after wild-type plasmid transfection NF-H₂O nuclease-free water

Primer & probe A: The primers and probes of FGFR3\TERT\ PLEKHS1\ATCB were mixed in a proper proportion to prepare primer & probe A.

Primer & probe B: The methylation detection primers and probes of OTX1\NRN1\NID2\ATCB were mixed in a proper proportion to prepare primer & probe B.

3. Reaction System and Detection Procedure of the Kit

The same sample was detected for point mutation and methylation respectively. That is, part of the nucleic acid in the same sample was carried out for heavy salt transformation according to the instructions of heavy salt transformation reagent (EZ DNA Methylation-Gold, Cat D5005), and part of nucleic acid was used for gene point mutation detection. Sample detection system was prepared as shown in the table below:

Gene point mutation detection reaction system (reaction tube A):

reagent name reaction volume (μL) Primer&Probe A 2 Hotstart HiTaq DNA polymerase 1 Hotstart HiTaq Buffer 24 PCR enhancer 1 nucleic acid to be detected 5 NF-H₂O 17 total volume 50

Gene methylation detection reaction system (reaction tube B):

the reaction volume reagent name (μL) Primer&Probe B 2 Hotstart HiTaq DNA polymerase 1 Hotstart HiTaq Buffer 24 PCR enhancer 1 purified nucleic acid after heavy 5 salt transformation NF-H₂O 17 total volume 50

The reaction system for the sample to be detected was prepared according to the above table, the reaction system was mixed uniformly by vortex, the reaction system after mixing was placed on a thermal cycler and was detected according to the following procedure:

the first stage 95° C. 10 min  1 cycle pre-denaturation the second stage 95° C. 15 s 15 cycles high TM template 59° C. 45 s enrichment 72° C.  1 min the third stage 95° C. 15 s 35 cycles 55° C. 45 s 72° C.  1 min collection of the fluorescence signal the fourth stage 40° C.  1 min  1 cycle cooling

4. Standards for Determination of Negative and Positive Results

The negative and positive was interpreted according to the following table:

standards for standards for determination determination standard for standard for of positive of negative detection category gene name positive results negative results results results point mutation FGFR3 Ct < 30.5 Ct > 30.5 The results of The results detection or no CT point mutation of point value test and mutation test TERT Ct < 28.5 Ct > 28.5 methylation and or no CT test are at least methylation value 1 positive, and test are both PLEKHS1 Ct < 30.5 Ct > 30.5 the sample is negative, the or no CT interpreted as sample is value positive. interpreted as ATCB Ct < 36 Ct < 36 negative. methylation OTX1 Ct < 30.5 Ct > 30.5 detection or no CT value NRN1 Ct < 28.5 Ct > 28.5 or no CT value NID2 Ct < 30.5 Ct > 30.5 or no CT value ATCB Ct < 36 Ct < 36

Example 2 Optimization of Primers and Probes of the Combined Auxiliary Diagnostic Kit of Gene Point Mutation and Methylation of the Bladder Cancer Driver Genes

The primers and probes combination and primer concentration for point mutation was screened and optimized according to the following table:

forward primer reverse primer probes primers and probes concentration concentration concentration gene combination gradient(μM) gradient (μM) gradient(μM) FGFR3 FGFR3-ARMS-F1; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 FGFR3-ARMS-R; FGFR3-ARMS-FAM; FGFR3-ARMS-F2; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 FGFR3-ARMS-R; FGFR3-ARMS-FAM; FGFR3-ARMS-F3; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 FGFR3-ARMS-R; FGFR3-ARMS-FAM; FGFR3-ARMS-F4 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 FGFR3-ARMS-R; FGFR3-ARMS-FAM; TERT TERT-ARMS-F1; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 TERT-ARMS-R; TERT-ARMS-HEX; TERT-ARMS-F2; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 TERT-ARMS-R; TERT-ARMS-HEX; TERT-ARMS-F3; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 TERT-ARMS-R; TERT-ARMS-HEX; TERT-ARMS-F4; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 TERT-ARMS-R; TERT-ARMS-HEX; PLEKHS1 PLEKHS1-ARMS-F1; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 PLEKHS1-ARMS-R; PLEKHS1-ARMS-ROX; PLEKHS1-ARMS-F2; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 PLEKHS1-ARMS-R; PLEKHS1-ARMS-ROX; PLEKHS1-ARMS-F3; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 PLEKHS1-ARMS-R; PLEKHS1-ARMS-ROX; PLEKHS1-ARMS-F4; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 PLEKHS1-ARMS-R; PLEKHS1-ARMS-ROX; ATCB ATCB-ARMS-F; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 ATCB-ARMS-R; ATCB-ARMS-VIC;

The primers and probes combination and the concentration of primers and probes for methylation was screened and optimized according to the following table:

forward reverse primers and probes primer concentration primer concentration probes concentration gene combination gradient(μM) gradient (μM) gradient(μM) OTX1 OTX1-BIS-F1; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 OTX1-BIS-R1; OTX1-BIS-FAM; OTX1-BIS-F2; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 OTX1-BIS-R1; OTX1-BIS-FAM; OTX1-BIS-F1; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 OTX1-BIS-R2; OTX1-BIS-FAM; OTX1-BIS-F2; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 OTX1-BIS-R2; OTX1-BIS-FAM; OTX1-BIS-F1; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 OTX1-BIS-R3; OTX1-BIS-FAM; OTX1-BIS-F2; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 OTX1-BIS-R3; OTX1-BIS-FAM; NRN1 NRN1-BIS-F1; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 NRN1-BIS-R1; NRN1-BIS-HEX; NRN1-BIS-F1; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 NRN1-BIS-R2; NRN1-BIS-HEX; NRN1-BIS-F1; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 NRN1-BIS-R3; NRN1-BIS-HEX; NID2 NID2-BIS-F1 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 NID2-BIS-R1 NID2-BIS-ROX; NID2-BIS-F1; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 NID2-BIS-R2; NID2-BIS-ROX; NID2-BIS-F1; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 NID2-BIS-R3; NID2-BIS-ROX; ATCB ATCB-BIS-F; 2.5/5/10/25/40/50 2.5/5/10/25/40/50 2.5/5/10/25/40 ATCB-BIS-R; ATCB-BIS-VIC;

According to Example 1, the reaction system was formulated, and the point mutation positive quality control product, methylation positive quality control product and negative control product were used as system test templates, and the primers and probes combination and concentration in the above table were tested respectively.

Test Result

Specific test results of primers and probes combination:

negative point control mutation product forward/ positive ( Whether reverse quality there is a primer probe control non-specific primers and probes amount amount product amplification gene combination (μM) (μM) ( Ct ) curve ) FGFR3 FGFR3-ARMS-F1; 10 5 22.4 None FGFR3-ARMS-R; FGFR3-ARMS-FAM; FGFR3-ARMS-F2; 10 5 22.8 Yes FGFR3-ARMS-R; FGFR3-ARMS-FAM; FGFR3-ARMS-F3; 10 5 23.3 Yes FGFR3-ARMS-R; FGFR3-ARMS-FAM; FGFR3-ARMS-F4; 10 5 21.3 None FGFR3-ARMS-R; FGFR3-ARMS-FAM; TERT TERT-ARMS-F1; 10 5 25.7 None TERT-ARMS-R; TERT-ARMS-HEX; TERT-ARMS-F2; 10 5 26.5 None TERT-ARMS-R; TERT-ARMS-HEX; TERT-ARMS-F3; 10 5 22.6 Yes TERT-ARMS-R; TERT-ARMS-HEX; TERT-ARMS-F4; 10 5 24.3 None TERT-ARMS-R; TERT-ARMS-HEX; PLEKHS1 PLEKHS1-ARMS-F1; 10 5 21.5 Yes PLEKHS1-ARMS-R; PLEKHS1-ARMS-ROX; PLEKHS1-ARMS-F2; 10 5 22.9 None PLEKHS1-ARMS-R; PLEKHS1-ARMS-ROX; PLEKHS1-ARMS-F3; 10 5 23.4 Yes PLEKHS1-ARMS-R; PLEKHS1-ARMS-ROX; PLEKHS1-ARMS-F4; 10 5 21.8 None PLEKHS1-ARMS-R; PLEKHS1-ARMS-ROX; ATCB ATCB-ARMS-F; 10 5 19.8 None ATCB-ARMS-R; ATCB-ARMS-VIC; negative control methylation product forward/ positive ( existence of a reverse quality non-specific primer probe control amplification primers and probes amount amount product curve: Yes or gene combination (μM) (μM) ( Ct ) None ) OTX1 OTX1-BIS-F1; 10 5 22.3 None OTX1-BIS-R1; OTX1-BIS-FAM; OTX1-BIS-F2; 10 5 24.5 Yes OTX1-BIS-R1; OTX1-BIS-FAM; OTX1-BIS-F1; 10 5 21.8 Yes OTX1-BIS-R2; OTX1-BIS-FAM; OTX1-BIS-F2; 10 5 23.4 None OTX1-BIS-R2; OTX1-BIS-FAM; OTX1-BIS-F1; 10 5 22.9 None OTX1-BIS-R3; OTX1-BIS-FAM; OTX1-BIS-F2; 10 5 23.9 None OTX1-BIS-R3; OTX1-BIS-FAM; NRN1 NRN1-BIS-F1; 10 5 21.3 Yes NRN1-BIS-R1; NRN1-BIS-HEX NRN1-BIS-F1; 10 5 24.7 None NRN1-BIS-R2; NRN1-BIS-HEX; NRN1-BIS-F1; 10 5 25.8 Yes NRN1-BIS-R3; NRN1-BIS-HEX; NID2 NID2-BIS-F1; 10 5 22.7 Yes NID2-BIS-R1; NID2-BIS-ROX; NID2-BIS-F1; 10 5 21.6 None NID2-BIS-R2; NID2-BIS-ROX; NID2-BIS-F1; 10 5 20.6 None NID2-BIS-R3; NID2-BIS-ROX; ATCB ATCB-BIS-F; 10 5 19.6 None ATCB-BIS-R; ATCB-BIS-VIC;

Comparison table of primers and probes concentration gradient test results:

point mutation positive negative quality control control product products (existence of forward reverse with non-specific primers and primer primer probes different products: probes concentration concentration concentration primer Yes or gene combination gradient(μM) gradient(μM) gradient(μM) concentrations (Ct) None) FGFR3 FGFR3-ARMS-F1; 2.5/5/10/ 2.5/5/10/ 10 2.5: 24.8  Yes, at FGFR3-ARMS-R; 25/40/50 25/40/50  5: 22.4 40/50 μM FGFR3-ARMS-FAM; 10: 21.9 25: 21.5 40: 21.2 50: 20.8 FGFR3-ARMS-F2; 2.5/5/10/ 2.5/5/10/ 10 2.5: 23.9  Yes, at FGFR3-ARMS-R; 25/40/50 25/40/50  5: 22.8 50 μM FGFR3-ARMS-FAM;  10: 22.02 25: 21.8 40: 20.8 50: 20.5 FGFR3-ARMS-F3; 2.5/5/10/ 2.5/5/10/ 10 2.5: 24.8  Yes, at FGFR3-ARMS-R; 25/40/50 25/40/50  5: 23.3 40/50 μM FGFR3-ARMS-FAM;  10: 22.15 25: 21.8 40: 21.5 50: 21.6 FGFR3-ARMS-F4; 2.5/5/10/ 2.5/5/10/ 10 2.5:     None FGFR3-ARMS-R; 25/40/50 25/40/50  5: 21.3 FGFR3-ARMS-FAM; 10: 20.8 25: 19.8 40: 20.5 50: 19.7 TERT TERT-ARMS-F1; 2.5/5/10/ 2.5/5/10/ 10 2.5: 28.7  Yes, at TERT-ARMS-R; 25/40/50 25/40/50  5: 25.7 10/25/40/50 μM TERT-ARMS-HEX; 10: 24.8 25: 24.5 40: 23.8 50: 22.9 TERT-ARMS-F2; 2.5/5/10/ 2.5/5/10/ 10 2.5: 28.9  Yes, at TERT-ARMS-R; 25/40/50 25/40/50  5: 26.5 25/40/50 μM TERT-ARMS-HEX; 10: 25.9 25: 25.1 40: 24.9 50: 24.5 TERT-ARMS-F3; 2.5/5/10/ 2.5/5/10/ 10 2.5: 24.8  Yes, at TERT-ARMS-R; 25/40/50 25/40/50  5: 22.6 25/40/50 μM TERT-ARMS-HEX; 10: 21.8 25: 21.5 40: 20.8 50: 19.8 TERT-ARMS-F4; 2.5/5/10/ 2.5/5/10/ 10 2.5: 26.9  Yes, at TERT-ARMS-R; 25/40/50 25/40/50  5: 24.3 50 μm TERT-ARMS-HEX; 10: 23.8 25: 23.5 40: 22.5 50: 22.0 PLEK PLEKHS1-ARMS-F1 2.5/5/10/ 2.5/5/10/ 10 2.5: 23.8  Yes, at HS1 PLEKHS1-ARMS-R; 25/40/50 25/40/50  5: 21.5 25/40/50 μM PLEKHS1-ARMS-ROX; 10: 20.5 25: 20.0 40: 19.5 50: 19.5 PLEKHS1-ARMS-F2 2.5/5/10/ 2.5/5/10/ 10 2.5: 25.5  Yes, at PLEKHS1-ARMS-R; 25/40/50 25/40/50  5: 22.9 25/40/50 μM PLEKHS1-ARMS-ROX; 10: 22.5 25: 20.5 40: 20.1 50: 19.5 PLEKHS1-ARMS-F3 2.5/5/10/ 2.5/5/10/ 10 2.5: 24.5  Yes, at PLEKHS1-ARMS-R; 25/40/50 25/40/50  5: 23.4 40/50 μM PLEKHS1-ARMS-ROX; 10: 22.5 25: 22.6 40: 21.8 50: 21.5 PLEKHS1-ARMS-F4 2.5/5/10/ 2.5/5/10/ 10 2.5: 24.0  None PLEKHS1-ARMS-R; 25/40/50 25/40/50  5: 21.8 PLEKHS1-ARMS-ROX; 10: 21.0 25: 20.5 40: 20.0 50: 19.5 ATCB ATCB-ARMS-F; 2.5/5/10/ 2.5/5/10/ 10 2.5: 21.5  None ATCB-ARMS-R; 25/40/50 25/40/50  5: 19.8 ATCB-ARMS-VIC; 10: 19.5 25: 19.0 40: 18.5 50: 18.0 Methylation positive negative quality control control product Forward/ products with (existence of reverse different a non-specific primers and primer probes primer amplification probes concentration concentration concentrations curve: Yes or gene combination gradient(μM) (μM) (Ct) None) OTX1 OTX1-BIS-F1; 2.5/5/10/ 10 2.5: 25.9  Yes, at OTX1-BIS-R1 25/40/50  5: 22.3 25/40/50 μM OTX1-BIS-FAM; 10: 21.8 25: 21.5 40: 21.0 50: 21.0 OTX1-BIS-F2; 2.5/5/10/ 10 2.5: 25.5  Yes, at OTX1-BIS-R1; 25/40/50  5: 24.5 25/40/50 μM OTX1-BIS-FAM; 10: 23.5 25: 23.2 40: 22.8 50: 22.5 OTX1-BIS-F1; 2.5/5/10/ 10 2.5: 23.6  Yes, at OTX1-BIS-R2; 25/40/50  5: 21.8 40/50 μM OTX1-BIS-FAM; 10: 21.5 25: 20.6 40: 20.1 50: 20.3 OTX1-BIS-F2; 2.5/5/10/ 10 2.5: 25.4  Yes, at OTX1-BIS-R2; 25/40/50  5: 23.4 450 μM OTX1-BIS-FAM; 10: 22.8 25: 22.0 40: 21.5 50: 21.0 OTX1-BIS-F1; 2.5/5/10/ 10 2.5: 23.5  None OTX1-BIS-R3; 25/40/50  5: 22.9 OTX1-BIS-FAM; 10: 21.0 25: 20.5 40: 20.0 50: 19.5 OTX1-BIS-F2; 2.5/5/10/ 10 2.5: 25.5  Yes, at OTX1-BIS-R3; 25/40/50  5: 23.9 40/50 μM OTX1-BIS-FAM; 10: 22.5 25: 22.0 40: 21.5 50: 21.0 NRN1 NRN1-BIS-F1; 2.5/5/10/ 10 2.5: 23.5  Yes, at NRN1-BIS-R1; 25/40/50  5: 21.3 40/50 μM NRN1-BIS-HEX; 10: 20.5 25: 20.0 40: 19.5 50: 19.0 NRN1-BIS-F1; 2.5/5/10/ 10 2.5: 25.8  Yes, at NRN1-BIS-R2; 25/40/50  5: 24.7 40/50 μM NRN1-BIS-HEX; 10: 22.5 25: 22.2 40: 22.0 50: 21.8 NRN1-BIS-F1; 2.5/5/10/ 10 2.5: 26.8  None NRN1-BIS-R3; 25/40/50  5: 25.8 NRN1-BIS-HEX; 10: 24.3 25: 23.5 40: 23.0 50: 22.5 NID2 NID2-BIS-F1; 2.5/5/10/ 10 2.5: 24.8  Yes, at NID2-BIS-R1; 25/40/50  5: 22.7 25/40/50 μM NID2-BIS-ROX; 10: 21.5 25: 21.0 40: 20.5 50: 20.0 NID2-BIS-F1; 2.5/5/10/ 10 2.5: 23.5  Yes, at NID2-BIS-R2; 25/40/50  5: 21.6 25/40/50 μM NID2-BIS-ROX; 10: 21.0 25: 20.5 40: 20.0 50: 20.3 NID2-BIS-F1; 2.5/5/10/ 10 2.5: 23.5  None NID2-BIS-R3; 25/40/50  5: 20.6 NID2-BIS-ROX; 10: 20.3 25: 19.5 40: 19.0 50: 18.9 ATCB ATCB-BIS-F; 2.5/5/10/ 10 2.5: 21.5  None ATCB-BIS-R; 25/40/50  5: 19.6 ATCB-BIS-VIC; 10: 19.5 25: 19.0 40: 18.5 50: 18.0

According to the comprehensive evaluation of primer specificity and amplification efficiency, the optimal primers and probes combination and concentration were shown in the following table:

primers and probes the amount of primers Gene combination and probes(μM) Primer& FGFR3 FGFR3-ARMS-F4: 25, 25, 15 Probe A FGFR3-ARMS-R; FGFR3-ARMS-FAM; TERT TERT-ARMS-F4; 25, 25, 10 TERT-ARMS-R: TERT-ARMS-HEX; PLEKHS1 PLEKHS1-ARMS-F4; 25, 25, 10 PLEKHS1-ARMS-R; PLEKHS1-ARMS-ROX; ATCB ATCB-ARMS-F; 2.5, 2.5, 5 ATCB-ARMS-R; ATCB-ARMS-VIC: Primer& OTX1 OTX1-BIS-F1; 25, 25.15 Probe B OTX1-BIS-R3; OTX1-BIS-FAM; NRN1 NRN1-BIS-F1; 25, 25, 15 NRN1-BIS-R2; NRN1-BIS-HEX; NID2 NID2-BIS-F1; 25, 25, 15 NID2-BIS-R3; NID2-BIS-ROX; ATCB ATCB-BIS-F; 2.5, 2.5, 5 ATCB-BIS-R; ATCB-BIS-VIC;

Example 3 Optimization of Reactive Enzymes and Detection Procedures of the Combined Auxiliary Diagnostic Kit of Gene Point Mutation and Methylation of the Bladder Cancer Driver Genes

Point mutation positive quality control products, methylation positive quality control products and negative quality control products were used as detection templates (10 replicates).

The optimization test of reactive enzymes and the detection procedures are respectively carried out according to the following table:

enzyme test point types of enzymes dosage (U) statistical method reactive Taq DNA polymerase, 1-100 The detection rate of enzymes HiFi Master Mix, Gold positive samples, Ct 360 Master Mix, 2 G value and false Robust Master Mix negative number of negative samples were counted.

test point test type result statistics detection standard qPCR The detection rate of procedures detection procedure positive samples, Ct value the detection procedure and false negative number of the present of negative samples were disclosure counted

The standard qPCR detection procedure was consisted of the first stage, the third stage and the fourth stage in Example 1.

Test Results

detection average Ct rate values of detection average Ct false of point point rate of values of negative mutation mutation methylation methylated number positive positive positive positive of quality quality quality quality negative DNA control control control control control polymerase products products products products products Taq DNA  75% 32.05  95% 26.5 4 polymerase HiFi Master 100% 29.05  90% 25.5 3 Mix Gold 360 100% 28.5 100% 29.5 0 Master Mix 2 G Robust  95% 30.5 100% 32 7 Master Mix

To sum up, the optimal reactive enzyme system was Gold 360 Master Mix.

false negative detection rate of detection rate of number of point mutation methylation negative detection procedures positive quality positive quality control type control products control products products standard qPCR 100%  85% 3 detection procedure the detection procedure 100% 100% 0 of the present disclosure

To sum up, the optimal reaction detection procedure was the detection procedure of the present disclosure.

Example 4 Detection Limit of the Combined Auxiliary Diagnostic Kit of Gene Point Mutation and Methylation of the Bladder Cancer Driver Genes

According to the following table, the point mutation positive plasmid (E10 UI) and the methylation positive plasmid (methylation level 100%) were verified by first-generation sequencing. The negative plasmid was a DNA plasmid (E10 UI) without the above-mentioned detected mutation and unmethylated, and the sample was diluted in gradient, and the quantitative standard curve of point mutation and the standard curve of methylation level were drawn.

methylation point positive point mutation mutation plasmid positive plasmid content (methylation dilution in gradient (UI/mL) level) statistical method high concentration E5 50% The positive medium E4 10% detection rate concentration E3  5% and repeatability low concentration E2 7.5%  at different 50  1% concentrations 10 0.5%  were counted respectively

According to the gradient dilution in the above table, the positive samples and negative samples with corresponding detection content were prepared, the samples were tested according to the optimal detection method (the parameters of the optimal detection method were as shown in the following table), and the theoretical detection value, actual detection value and CV of positive samples were counted.

The optimal detection reaction system was as follows:

Point mutation reaction system:

dosage volume or component primer or reagent name amount of substance PCR Mix 2 × Gold 360 Master Mix 25 μL Probe/primer FGFR3-ARMS-F4 25 μM Mix FGFR3-ARMS-R 25 μM FGFR3-ARMS-FAM 15 μM TERT-ARMS-F4 25 μM TERT-ARMS-R 25 μM TERT-ARMS-HEX 10 μM PLEKHS1-ARMS-F4 25 μM PLEKHS1-ARMS-R 25 μM PLEKHS1-ARMS-ROX 10 μM ATCB-ARMS-F 2.5 μM ATCB-ARMS-R 2.5 μM ATCB-ARMS-VIC 5 μM PCR enhancer 25 × PCR enhancer 2 μL products to be purified nucleic acid product 5 μL tested NF—H₂O NF—H₂O make up to 50 μL

Gene methylation reaction system:

dosage volume or component primer or reagent name amount of substance PCR Mix 2 × Gold 360 Master Mix 25 μL Probe/primer OTX1-ARMS-F1 25 μM Mix OTX1-ARMS-R3 25 μM OTX1-ARMS-FAM 15 μM NRN1-ARMS-F1 25 μM NRN1-ARMS-R2 25 μM NRN1-ARMS-HEX 10 μM NID2-ARMS-F1 25 μM NID2-ARMS-R3 25 μM NID2-ARMS-ROX 10 μM ATCB-ARMS-F 2.5 μM ATCB-ARMS-R 2.5 μM ATCB-ARMS-VIC 5 μM PCR enhancer 25 × PCR enhancer 2 μL products to be tested purified nucleic acid product 5 μL NF—H₂O NF—H₂O make up to 50 μL

Optimal detection reaction procedure:

the first stage 95° C. 10 min 1 cycle pre-denaturation the second 95° C. 15 s 15 cycles high TM template stage 59° C. 45 s enrichment 72° C. 1 min the third 95° C. 15 s 35 cycles stage 55° C. 45 s 72° C. 1 min collection of the fluorescence signal the fourth stage 40° C. 1 min 1 cycle cooling

Standards for determination of negative and positive results:

standards for standards for standards for determination determination detection gene positive standards for of positive of negative category name results negative results results results point FGFR3 Ct < 30.5 Ct > 30.5 or no The results of The results of mutation Ct value point mutation point mutation detection TERT Ct < 28.5 Ct > 28.5 or no test and test and Ct value methylation methylation PLEKHS1 Ct < 30.5 Ct > 30.5 or no test are at test are both Ct value least 1 negative, the ATCB Ct < 36  Ct < 36 positive, and sample is methylation OTX1 Ct < 30.5 Ct > 30.5 or no the sample is interpreted detection Ct value interpreted as as negative. NRN1 Ct < 28.5 Ct > 28.5 or no positive. Ct value NID2 Ct < 30.5 Ct > 30.5 or no Ct value ATCB Ct < 36  Ct < 36

Test Results

theoretical theoretical methylation value of point level of mutation methylation- positive actual test positive actual test standard content CV % standard content CV % 1E5 0.98E5 0.3 50% 49.75% 0.1 1E4 0.97E4 0.5 10% 9.88% 0.4 1E3 0.99E3 0.8  5% 4.88% 0.6 1E2 0.97E2 1.0 2.5%  2.03% 1.0 50 49.88 1.5  1% 0.91% 1.2 10 — — 0.5%  0.47% 2.0

Example 5 Clinical Trial of the Combined Auxiliary Diagnostic Kit of Gene Point Mutation and Methylation of the Bladder Cancer Driver Genes

According to the requirements of clinical trials, 100 cases (53 cases with negative hematuria and 47 cases with positive hematuria) were obtained. Nucleic acid extraction was carried out on urine precipitation samples respectively by using the nucleic acid extraction kits, and 100 ng of urine precipitation nucleic acids were taken for heavy salt transformation (see the instructions for heavy salt transformation operation). 100 clinical samples were tested according to the above-mentioned optimal detection methods (negative and positive interpretation standards in Example 1, the best primers and probes combination in Example 2, and the best detection reaction system in Example 3). The number of true positive, true negative, false positive and false negative samples were counted respectively, and the corresponding specificity and sensitivity performance were counted.

Test Results

Point mutation test results:

true false true false positive negative negative positive pathological 47 40 7 positive sample pathological 53 48 5 negative sample

Gene methylation test results:

specificity sensitivity positive predictive negative predictive (%) (%) value (%) value (%) 85.10 90.56 88.88 87.27

true false true false positive negative negative positive pathological 47 38 9 positive sample pathologically 53 53 0 negative sample

specificity sensitivity positive predictive negative predictive (%) (%) value (%) value (%) 80.85 100 100 85.48

Point mutation and gene methylation combined test results:

true false true false positive negative negative positive Pathological 47 43 4 positive sample Pathologically 53 53 0 negative sample

specificity sensitivity positive predictive negative predictive (%) (%) value (%) value (%) 91.48 100 100 92.98

The above-mentioned is only to explain some embodiments of the present disclosure. Since it is easy for those ordinary technicians in the same technical field to make a number of modifications and changes on this basis, the present disclosure is not intended to limit the present invention to the specific structure, method steps and scope of application shown and described. Therefore, all the corresponding modifications and equivalents that may be utilized belong to the scope of patent applications for the present invention. 

1. A detection reagent for screening bladder cancer by targeting genes related to the pathway of bladder cancer, comprising specific primers and probes designed for a template of a region to be detected, wherein the region to be detected comprises a combination of gene point mutation and gene methylation; wherein the gene point mutation comprises a point mutation for one or more combinations of FGFR3, TERT and PLEKHS1; wherein the gene methylation comprises methylation for one or more combinations of OTX1, NID2 and NRN1; wherein the region to be detected for FGFR3 point mutation is the sequence set forth in SEQ ID NO: 1; the region to be detected for TERT point mutation is the sequence set forth in SEQ ID NO: 2; the region to be detected for PLEKHS1 point mutation is the sequence set forth in SEQ ID NO: 3; wherein the region to be detected for OTX1 methylation is the sequence set forth in SEQ ID NO: 4; the region to be detected for NID2 methylation is the sequence set forth in SEQ ID NO: 5; the region to be detected for NRN1 methylation is the sequence set forth in SEQ ID NO:
 6. 2-12. (canceled)
 13. The detection reagent according to claim 1, wherein the probe is selected from any sequence set forth in SEQ ID NOs: 12, 18, 24, 30, 35 and 40 or a combination thereof.
 14. The detection reagent according to claim 1, wherein the specific primers designed for the template of the region to be detected are selected from one or more combinations of the following primer pairs: the forward primers and reverse primers for FGFR3 point mutation are selected from any sequence set forth in SEQ ID NOs: 7-10 as well as the sequence set forth in SEQ ID NO: 11; and/or the forward primers and reverse primers for TERT point mutation are selected from any sequence set forth in SEQ ID NOs: 13-16 as well as the sequence set forth in SEQ ID NO: 17; and/or the forward primers and reverse primers for PLEKHS1 point mutation are selected from any sequence set forth in SEQ ID NOs: 19-22 as well as the sequence set forth in SEQ ID NO: 23; and/or the forward primers and reverse primers for OTX1 methylation are selected from any sequence set forth in SEQ ID NOs: 25 and 26 and any sequence set forth in SEQ ID NOs: 27-29; and/or the forward primers and reverse primers for NID2 methylation are selected from the sequence set forth in SEQ ID NO: 31 as well as any sequence set forth in SEQ ID NOs: 32-34; and/or the forward primers and reverse primers for NRN1 methylation are selected from the sequence set forth in SEQ ID NO: 36 as well as any sequence set forth in SEQ ID NO: 37-39.
 15. The detection reagent according to claim 1, wherein the specific primers designed for the template of the region to be detected are selected from one or more combinations of the following primer pairs: the forward primers and reverse primers for FGFR3 point mutation are the sequences set forth in SEQ ID NOs: 10 and 11, respectively; and/or the forward primers and reverse primers for TERT point mutation are the sequences set forth in SEQ ID NOs: 16 and 17 respectively; and/or the forward primers and reverse primers for PLEKHS1 point mutation are the sequences set forth in SEQ ID NOs: 22 and 23, respectively; and/or the forward primers and reverse primers for OTX1 methylation are the sequences set forth in SEQ ID NOs: 25 and 29, respectively; and/or the forward primers and reverse primers for NID2 methylation are the sequences set forth in SEQ ID NOs: 31 and 34, respectively; and/or the forward primers and reverse primers for NRN1 methylation are the sequences set forth in SEQ ID NOs: 36 and 39, respectively.
 16. The detection reagent according to claim 1, wherein the specific primers and probes designed for the template of the region to be detected are selected from one or more combinations of the following primer pairs and probes: the forward primer and reverse primer and probe for FGFR3 point mutation are the sequences set forth in SEQ ID NOs: 10, 11 and 12, respectively; and/or the forward primer and reverse primer and probe for TERT point mutation are the sequences set forth in SEQ ID NOs: 16, 17 and 18, respectively; and/or the forward primer and reverse primer and probe for PLEKHS1 point mutation are the sequences set forth in SEQ ID NOs: 22, 23 and 24, respectively; and/or the forward primer and reverse primer and probe for OTX1 methylation are the sequences set forth in SEQ ID NOs: 25, 29 and 30, respectively; and/or the forward primer and reverse primer and probe for NID2 methylation are the sequences set forth in SEQ ID NOs: 31, 34 and 35, respectively; and/or the forward primer and reverse primer and probe for NRN1 methylation are the sequences set forth in SEQ ID NOs: 36, 39 and 40 respectively.
 17. (canceled)
 18. The detection reagent according to claim 1, further comprising primers and probes designed for an internal reference gene, wherein the internal reference gene is ATCB; wherein the primers and probes designed for the internal reference gene are the sequences set forth in SEQ ID NOs:41-43. 19-24. (canceled)
 25. The detection reagent according to claim 1, wherein primers and probes for point mutations and methylation levels are further distributed in different reaction tubes, the reaction tubes are respectively a reaction tube A and a reaction tube B, wherein, the reaction tube A is used to detect point mutation, and a composition thereof is as follows: reagent name reaction volume (μL) Primer&Probe A 2 2 × Gold 360 Master Mix 25 PCR enhancer 1 nucleic acid to be detected 5 NF—H₂O 17 total volume 50

wherein, Primer&Probe A is a mixture composed of three driver genes point mutations of FGFR3\TERT\PLEKHS1 and internal reference primers and probes; wherein, the reaction tube B is used to detect methylation, and the composition is as follows: reagent name the reaction volume (μL) Primer&Probe B 2 2 × Gold 360 Master Mix 25 PCR enhancer 1 purified nucleic acid after heavy salt 5 transformation NF—H₂O 17 total volume 50

wherein, Primer&Probe B is a mixture composed of three driver genes methylation of OTX1\NRN1\NID2 and internal reference primers and probes.
 26. The detection reagent according to claim 1, comprising the following components: reagent name main components primer&probe A mixture of three driver genes point mutations of FGFR3, TERT, PLEKHS1 and internal reference primers and probes primer&probe B mixture of three driver genes methylation of OTX1, NRN1, NID2 and internal reference primers and probes DNA polymerase DNA polymerase, dNTPs, Mg²⁺, Tris-HCl, NaCl and Master Mix Nuclease-free Water PCR enhancer DTT and/or BSA point mutation adenovirus packaging positive mutant plasmid positive quality control methylation methylation-positive nucleic acid after methylase positive quality transformation control negative control T cells after wild-type plasmid transfection NF—H₂O nuclease-free water

wherein the sequences and concentration of each primer pair and probe in primer & probe A are as follows: the forward primer, reverse primer and probe for FGFR3 point mutation are the sequences set forth in SEQ ID NOs: 10, 11 and 12, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward prime, reverse primer and probe for TERT point mutation are the sequences set forth in SEQ ID NOs: 16, 17 and 18, and the concentrations are 25 μM, 25 μM and 10 μM respectively; the forward primer, reverse primer and probe for PLEKHS1 point mutation are the sequences set forth in SEQ ID NOs: 22, 23 and 24, and the concentrations are 25 μM, 25 μM and 8 μM respectively; the forward primer, reverse primer and probe for the internal reference gene are the sequences set forth in SEQ ID NOs: 41, 42 and 43, and the concentrations are 2.5 μM, 2.5 μM and 5 μM respectively; wherein the sequences and concentration of each primer pair and probe in primer & probe B are as follows: the forward primer, reverse primer and probe for OTX1 methylation are the sequences set forth in SEQ ID NOs: 25, 29 and 30, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe for NID2 methylation are the sequences set forth in SEQ ID NOs: 31, 34 and 35, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe for NRN1 methylation are the sequences set forth in SEQ ID NOs: 36, 39 and 40, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe the internal reference gene are the sequences set forth in SEQ ID NOs: 41-43, and the concentrations are 2.5 μM, 2.5 μM and 5 μM, respectively. 27-35. (canceled)
 36. The detection reagent according to claim 13, wherein primers and probes for point mutations and methylation levels are further distributed in different reaction tubes, the reaction tubes are respectively a reaction tube A and a reaction tube B, wherein, the reaction tube A is used to detect point mutation, and a composition thereof is as follows: reagent name reaction volume (μL) Primer&Probe A 2 2 × Gold 360 Master Mix 25 PCR enhancer 1 nucleic acid to be detected 5 NF—H₂O 17 total volume 50

wherein, Primer&Probe A is a mixture composed of three driver genes point mutations of FGFR3\TERT\PLEKHS1 and internal reference primers and probes; wherein, the reaction tube B is used to detect methylation, and the composition is as follows: the reaction volume reagent name (μL) Primer&Probe B 2 2 × Gold 360 Master Mix 25 PCR enhancer 1 purified nucleic acid after heavy salt 5 transformation NF—H₂O 17 total volume 50

wherein, Primer&Probe B is a mixture composed of three driver genes methylation of OTX1\NRN1\NID2 and internal reference primers and probes.
 37. The detection reagent according to claim 14, wherein primers and probes for point mutations and methylation levels are further distributed in different reaction tubes, the reaction tubes are respectively a reaction tube A and a reaction tube B, wherein, the reaction tube A is used to detect point mutation, and a composition thereof is as follows: reagent name reaction volume (μL) Primer&Probe A 2 2 × Gold 360 Master Mix 25 PCR enhancer 1 nucleic acid to be detected 5 NF—H₂O 17 total volume 50

wherein, Primer&Probe A is a mixture composed of three driver genes point mutations of FGFR3\TERT\PLEKHS1 and internal reference primers and probes; wherein, the reaction tube B is used to detect methylation, and the composition is as follows: the reaction volume reagent name (μL) Primer&Probe B 2 2 × Gold 360 Master Mix 25 PCR enhancer 1 purified nucleic acid after heavy salt 5 transformation NF—H₂O 17 total volume 50

wherein, Primer&Probe B is a mixture composed of three driver genes methylation of OTX1\NRN1\NID2 and internal reference primers and probes.
 38. The detection reagent according to claim 15, wherein primers and probes for point mutations and methylation levels are further distributed in different reaction tubes, the reaction tubes are respectively a reaction tube A and a reaction tube B, wherein, the reaction tube A is used to detect point mutation, and a composition thereof is as follows: reagent name reaction volume (μL) Primer&Probe A 2 2 × Gold 360 Master Mix 25 PCR enhancer 1 nucleic acid to be detected 5 NF—H₂O 17 total volume 50

wherein, Primer&Probe A is a mixture composed of three driver genes point mutations of FGFR3\TERT\PLEKHS1 and internal reference primers and probes; wherein, the reaction tube B is used to detect methylation, and the composition is as follows: the reaction volume reagent name (μL) Primer&Probe B 2 2 × Gold 360 Master Mix 25 PCR enhancer 1 purified nucleic acid after heavy salt 5 transformation NF—H₂O 17 total volume 50

wherein, Primer&Probe B is a mixture composed of three driver genes methylation of OTX1\NRN1\NID2 and internal reference primers and probes.
 39. The detection reagent according to claim 16, wherein primers and probes for point mutations and methylation levels are further distributed in different reaction tubes, the reaction tubes are respectively a reaction tube A and a reaction tube B, wherein, the reaction tube A is used to detect point mutation, and a composition thereof is as follows: reagent name reaction volume (μL) Primer&Probe A 2 2 × Gold 360 Master Mix 25 PCR enhancer 1 nucleic acid to be detected 5 NF—H₂O 17 total volume 50

wherein, Primer&Probe A is a mixture composed of three driver genes point mutations of FGFR3\TERT\PLEKHS1 and internal reference primers and probes; wherein, the reaction tube B is used to detect methylation, and the composition is as follows: the reaction volume reagent name (μL) Primer&Probe B 2 2 × Gold 360 Master Mix 25 PCR enhancer 1 purified nucleic acid after heavy salt 5 transformation NF—H₂O 17 total volume 50

wherein, Primer&Probe B is a mixture composed of three driver genes methylation of OTX1\NRN1\NID2 and internal reference primers and probes.
 40. The detection reagent according to claim 18, wherein primers and probes for point mutations and methylation levels are further distributed in different reaction tubes, the reaction tubes are respectively a reaction tube A and a reaction tube B, wherein, the reaction tube A is used to detect point mutation, and a composition thereof is as follows: reagent name reaction volume (μL) Primer&Probe A 2 2 × Gold 360 Master Mix 25 PCR enhancer 1 nucleic acid to be detected 5 NF—H₂O 17 total volume 50

wherein, Primer&Probe A is a mixture composed of three driver genes point mutations of FGFR3\TERT\PLEKHS1 and internal reference primers and probes; wherein, the reaction tube B is used to detect methylation, and the composition is as follows: the reaction volume reagent name (μL) Primer&Probe B 2 2 × Gold 360 Master Mix 25 PCR enhancer 1 purified nucleic acid after heavy salt 5 transformation NF—H₂O 17 total volume 50

wherein, Primer&Probe B is a mixture composed of three driver genes methylation of OTX1\NRN1\NID2 and internal reference primers and probes.
 41. The detection reagent according to claim 13, comprising the following components: reagent name main components primer&probe A mixture of three driver genes point mutations of FGFR3, TERT, PLEKHS1 and internal reference primers and probes primer&probe B mixture of three driver genes methylation of OTX1, NRN1, NID2 and internal reference primers and probes DNA polymerase DNA polymerase, dNTPs, Mg²⁺, Tris-HCl, NaCl and Master Mix Nuclease-free Water PCR enhancer DTT and/or BSA point mutation adenovirus packaging positive mutant plasmid positive quality control methylation methylation-positive nucleic acid after methylase positive quality transformation control negative control T cells after wild-type plasmid transfection NF—H₂O nuclease-free water

wherein the sequences and concentration of each primer pair and probe in primer & probe A are as follows: the forward primer, reverse primer and probe for FGFR3 point mutation are the sequences set forth in SEQ ID NOs: 10, 11 and 12, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward prime, reverse primer and probe for TERT point mutation are the sequences set forth in SEQ ID NOs: 16, 17 and 18, and the concentrations are 25 μM, 25 μM and 10 μM respectively; the forward primer, reverse primer and probe for PLEKHS1 point mutation are the sequences set forth in SEQ ID NOs: 22, 23 and 24, and the concentrations are 25 μM, 25 μM and 8 μM respectively; the forward primer, reverse primer and probe for the internal reference gene are the sequences set forth in SEQ ID NOs: 41, 42 and 43, and the concentrations are 2.5 μM, 2.5 μM and 5 μM respectively; wherein the sequences and concentration of each primer pair and probe in primer & probe B are as follows: the forward primer, reverse primer and probe for OTX1 methylation are the sequences set forth in SEQ ID NOs: 25, 29 and 30, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe for NID2 methylation are the sequences set forth in SEQ ID NOs: 31, 34 and 35, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe for NRN1 methylation are the sequences set forth in SEQ ID NOs: 36, 39 and 40, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe the internal reference gene are the sequences set forth in SEQ ID NOs: 41-43, and the concentrations are 2.5 μM, 2.5 μM and 5 μM, respectively.
 42. The detection reagent according to claim 14, comprising the following components: reagent name main components primer&probe A mixture of three driver genes point mutations of FGFR3, TERT, PLEKHS1 and internal reference primers and probes primer&probe B mixture of three driver genes methylation of OTX1, NRN1, NID2 and internal reference primers and probes DNA polymerase DNA polymerase, dNTPs, Mg²⁺, Tris-HCl, NaCl and Master Mix Nuclease-free Water PCR enhancer DTT and/or BSA point mutation adenovirus packaging positive mutant plasmid positive quality control methylation methylation-positive nucleic acid after methylase positive quality transformation control negative control T cells after wild-type plasmid transfection NF—H₂O nuclease-free water

wherein the sequences and concentration of each primer pair and probe in primer & probe A are as follows: the forward primer, reverse primer and probe for FGFR3 point mutation are the sequences set forth in SEQ ID NOs: 10, 11 and 12, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward prime, reverse primer and probe for TERT point mutation are the sequences set forth in SEQ ID NOs: 16, 17 and 18, and the concentrations are 25 μM, 25 μM and 10 μM respectively; the forward primer, reverse primer and probe for PLEKHS1 point mutation are the sequences set forth in SEQ ID NOs: 22, 23 and 24, and the concentrations are 25 μM, 25 μM and 8 μM respectively; the forward primer, reverse primer and probe for the internal reference gene are the sequences set forth in SEQ ID NOs: 41, 42 and 43, and the concentrations are 2.5 μM, 2.5 μM and 5 μM respectively; wherein the sequences and concentration of each primer pair and probe in primer & probe B are as follows: the forward primer, reverse primer and probe for OTX1 methylation are the sequences set forth in SEQ ID NOs: 25, 29 and 30, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe for NID2 methylation are the sequences set forth in SEQ ID NOs: 31, 34 and 35, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe for NRN1 methylation are the sequences set forth in SEQ ID NOs: 36, 39 and 40, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe the internal reference gene are the sequences set forth in SEQ ID NOs: 41-43, and the concentrations are 2.5 μM, 2.5 μM and 5 μM, respectively.
 43. The detection reagent according to claim 15, comprising the following components: reagent name main components primer&probe A mixture of three driver genes point mutations of FGFR3, TERT, PLEKHS1 and internal reference primers and probes primer&probe B mixture of three driver genes methylation of OTX1, NRN1, NID2 and internal reference primers and probes DNA polymerase DNA polymerase, dNTPs, Mg²⁺, Tris-HCl, NaCl and Master Mix Nuclease-free Water PCR enhancer DTT and/or BSA point mutation adenovirus packaging positive mutant plasmid positive quality control methylation methylation-positive nucleic acid after methylase positive quality transformation control negative control T cells after wild-type plasmid transfection NF—H₂O nuclease-free water

wherein the sequences and concentration of each primer pair and probe in primer & probe A are as follows: the forward primer, reverse primer and probe for FGFR3 point mutation are the sequences set forth in SEQ ID NOs: 10, 11 and 12, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward prime, reverse primer and probe for TERT point mutation are the sequences set forth in SEQ ID NOs: 16, 17 and 18, and the concentrations are 25 μM, 25 μM and 10 μM respectively; the forward primer, reverse primer and probe for PLEKHS1 point mutation are the sequences set forth in SEQ ID NOs: 22, 23 and 24, and the concentrations are 25 μM, 25 μM and 8 μM respectively; the forward primer, reverse primer and probe for the internal reference gene are the sequences set forth in SEQ ID NOs: 41, 42 and 43, and the concentrations are 2.5 μM, 2.5 μM and 5 μM respectively; wherein the sequences and concentration of each primer pair and probe in primer & probe B are as follows: the forward primer, reverse primer and probe for OTX1 methylation are the sequences set forth in SEQ ID NOs: 25, 29 and 30, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe for NID2 methylation are the sequences set forth in SEQ ID NOs: 31, 34 and 35, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe for NRN1 methylation are the sequences set forth in SEQ ID NOs: 36, 39 and 40, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe the internal reference gene are the sequences set forth in SEQ ID NOs: 41-43, and the concentrations are 2.5 μM, 2.5 μM and 5 μM, respectively.
 44. The detection reagent according to claim 16, comprising the following components: reagent name main components primer&probe A mixture of three driver genes point mutations of FGFR3, TERT, PLEKHS1 and internal reference primers and probes primer&probe B mixture of three driver genes methylation of OTX1, NRN1, NID2 and internal reference primers and probes DNA polymerase DNA polymerase, dNTPs, Mg²⁺, Tris-HCl, NaCl and Master Mix Nuclease-free Water PCR enhancer DTT and/or BSA point mutation adenovirus packaging positive mutant plasmid positive quality control methylation methylation-positive nucleic acid after methylase positive quality transformation control negative control T cells after wild-type plasmid transfection NF—H₂O nuclease-free water

wherein the sequences and concentration of each primer pair and probe in primer & probe A are as follows: the forward primer, reverse primer and probe for FGFR3 point mutation are the sequences set forth in SEQ ID NOs: 10, 11 and 12, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward prime, reverse primer and probe for TERT point mutation are the sequences set forth in SEQ ID NOs: 16, 17 and 18, and the concentrations are 25 μM, 25 μM and 10 μM respectively; the forward primer, reverse primer and probe for PLEKHS1 point mutation are the sequences set forth in SEQ ID NOs: 22, 23 and 24, and the concentrations are 25 μM, 25 μM and 8 μM respectively; the forward primer, reverse primer and probe for the internal reference gene are the sequences set forth in SEQ ID NOs: 41, 42 and 43, and the concentrations are 2.5 μM, 2.5 μM and 5 μM respectively; wherein the sequences and concentration of each primer pair and probe in primer & probe B are as follows: the forward primer, reverse primer and probe for OTX1 methylation are the sequences set forth in SEQ ID NOs: 25, 29 and 30, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe for NID2 methylation are the sequences set forth in SEQ ID NOs: 31, 34 and 35, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe for NRN1 methylation are the sequences set forth in SEQ ID NOs: 36, 39 and 40, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe the internal reference gene are the sequences set forth in SEQ ID NOs: 41-43, and the concentrations are 2.5 μM, 2.5 μM and 5 μM, respectively.
 45. The detection reagent according to claim 18, comprising the following components: reagent name main components primer&probe A mixture of three driver genes point mutations of FGFR3, TERT, PLEKHS1 and internal reference primers and probes primer&probe B mixture of three driver genes methylation of OTX1, NRN1, NID2 and internal reference primers and probes DNA polymerase DNA polymerase, dNTPs, Mg²⁺, Tris-HCl, NaCl and Master Mix Nuclease-free Water PCR enhancer DTT and/or BSA point mutation adenovirus packaging positive mutant plasmid positive quality control methylation methylation-positive nucleic acid after methylase positive quality transformation control negative control T cells after wild-type plasmid transfection NF—H₂O nuclease-free water

wherein the sequences and concentration of each primer pair and probe in primer & probe A are as follows: the forward primer, reverse primer and probe for FGFR3 point mutation are the sequences set forth in SEQ ID NOs: 10, 11 and 12, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward prime, reverse primer and probe for TERT point mutation are the sequences set forth in SEQ ID NOs: 16, 17 and 18, and the concentrations are 25 μM, 25 μM and 10 μM respectively; the forward primer, reverse primer and probe for PLEKHS1 point mutation are the sequences set forth in SEQ ID NOs: 22, 23 and 24, and the concentrations are 25 μM, 25 μM and 8 μM respectively; the forward primer, reverse primer and probe for the internal reference gene are the sequences set forth in SEQ ID NOs: 41, 42 and 43, and the concentrations are 2.5 μM, 2.5 μM and 5 μM respectively; wherein the sequences and concentration of each primer pair and probe in primer & probe B are as follows: the forward primer, reverse primer and probe for OTX1 methylation are the sequences set forth in SEQ ID NOs: 25, 29 and 30, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe for NID2 methylation are the sequences set forth in SEQ ID NOs: 31, 34 and 35, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe for NRN1 methylation are the sequences set forth in SEQ ID NOs: 36, 39 and 40, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe the internal reference gene are the sequences set forth in SEQ ID NOs: 41-43, and the concentrations are 2.5 μM, 2.5 μM and 5 μM, respectively.
 46. The detection reagent according to claim 25, comprising the following components: reagent name main components primer&probe A mixture of three driver genes point mutations of FGFR3, TERT, PLEKHS1 and internal reference primers and probes primer&probe B mixture of three driver genes methylation of OTX1, NRN1, NID2 and internal reference primers and probes DNA polymerase DNA polymerase, dNTPs, Mg²⁺, Tris-HCl, NaCl and Master Mix Nuclease-free Water PCR enhancer DTT and/or BSA point mutation adenovirus packaging positive mutant plasmid positive quality control methylation methylation-positive nucleic acid after methylase positive quality transformation control negative control T cells after wild-type plasmid transfection NF—H₂O nuclease-free water

wherein the sequences and concentration of each primer pair and probe in primer & probe A are as follows: the forward primer, reverse primer and probe for FGFR3 point mutation are the sequences set forth in SEQ ID NOs: 10, 11 and 12, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward prime, reverse primer and probe for TERT point mutation are the sequences set forth in SEQ ID NOs: 16, 17 and 18, and the concentrations are 25 μM, 25 μM and 10 μM respectively; the forward primer, reverse primer and probe for PLEKHS1 point mutation are the sequences set forth in SEQ ID NOs: 22, 23 and 24, and the concentrations are 25 μM, 25 μM and 8 μM respectively; the forward primer, reverse primer and probe for the internal reference gene are the sequences set forth in SEQ ID NOs: 41, 42 and 43, and the concentrations are 2.5 μM, 2.5 μM and 5 μM respectively; wherein the sequences and concentration of each primer pair and probe in primer & probe B are as follows: the forward primer, reverse primer and probe for OTX1 methylation are the sequences set forth in SEQ ID NOs: 25, 29 and 30, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe for NID2 methylation are the sequences set forth in SEQ ID NOs: 31, 34 and 35, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe for NRN1 methylation are the sequences set forth in SEQ ID NOs: 36, 39 and 40, and the concentrations are 25 μM, 25 μM and 15 μM respectively; the forward primer, reverse primer and probe the internal reference gene are the sequences set forth in SEQ ID NOs: 41-43, and the concentrations are 2.5 μM, 2.5 μM and 5 μM, respectively. 